A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3938994



Internal ID21359063
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:169178281..169178333hg38UCSC Ensembl
chr4:170099432..170099484hg19UCSC Ensembl
Cytoband4q32.3
Allele length
AssemblyAllele length
hg3853
hg1953
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15195703
SamplesHG002
Known GenesSH3RF1
MethodSequencing
Analysis
Platform
Comments
ReferenceWenger_et_al_2019
Pubmed ID31406327
Accession Number(s)nsv3938994
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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